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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1881353Generated: November 1, 2026

Water → 2-Hydroxy-5-nitroindane

https://huagongshe.com/reaction/1881353

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
Reactant5-Nitro-2-indanoneHCID 1502066—
ReactantSodium borohydrideHCID 4311764—
SolventIsopropanol ethanolHCID 22179027—
Product2-Hydroxy-5-nitroindaneHCID 368592783.2%

Reaction Steps

5-nitro-2-indanone (5.3 g, 30 mmol) was dissolved in EtOH: i-PrOH (1:1, 150 mL). NaBH4 (1.7 g, 45 mmol) was added portion by portion at room temperature. The reaction mixture was stirred at r.t for additional 30 min and water was added at 0° C. (ice-water bath). The reaction mixture was extracted with EtOAc (100 mL×3) and the combined organic layers were washed with water and brine and dried over Na2SO4. Purification of the concentrated crude product by column chromatography (EtOAc:Hexane=4:6) afforded the title product as a pale yellow oil (4.47 g, 83%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08318790B2
Source datasetuspto-grants-2012_11
ORD IDord-943281951add4b10a35157f9b1f2a570
Source noteuspto-grants-2012_11